blau syndrome Gene Set
| Dataset |
GAD Gene-Disease Associations
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| Category |
disease or phenotype associations
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| Type |
disease |
| Description |
An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas caused_by NOD2/CARD15 mutations. (Human Disease Ontology, DOID_0050678)
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| Similar Terms |
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| Downloads & Tools |
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Genes
1 genes associated with the disease blau syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
| Symbol |
Name |
|
NOD2
|
nucleotide-binding oligomerization domain containing 2
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